<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>NISCAIR Online Periodicals Repository Collection: IJC-B Vol.51B(01) [January 2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13375</link>
    <description />
    <textInput>
      <title>The Collection's search engine</title>
      <description>Search the Channel</description>
      <name>search</name>
      <link>http://nopr.niscair.res.in/simple-search</link>
    </textInput>
    <item>
      <title>Microwave assisted synthesis and antibacterial properties of some new 2-alkyl/aryl-(6-substitutedcoumarin-3-yl)imidazo[2,1-&lt;i style="mso-bidi-font-style: normal"&gt;b&lt;/i&gt;][1,3,4]thiadiazoles</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13405</link>
      <description>Title: Microwave assisted synthesis and antibacterial properties of some new 2-alkyl/aryl-(6-substitutedcoumarin-3-yl)imidazo[2,1-&lt;i style="mso-bidi-font-style: normal"&gt;b&lt;/i&gt;][1,3,4]thiadiazoles
&lt;br/&gt;
&lt;br/&gt;Authors: Jakhar, Anshu; Makrandi, J K
&lt;br/&gt;
&lt;br/&gt;Abstract: A series of&#xD;
2-alkyl/aryl-(6-substitutedcoumarin-3-yl)imidazo[2,1-&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;b&lt;/i&gt;][1,3,4] thiadiazoles &lt;b style="mso-bidi-font-weight:normal"&gt;3a-o&lt;/b&gt;&#xD;
have been synthesized by reacting 3-(2-bromoacetyl)-6-substitutedcoumarins &lt;b style="mso-bidi-font-weight:normal"&gt;1&lt;/b&gt; with various&#xD;
5-alkyl/aryl-2-amino-1,3,4-thiadiazoles &lt;b style="mso-bidi-font-weight:normal"&gt;2&lt;/b&gt;&#xD;
under normal thermal condition as well as microwave irradiation. The latter&#xD;
condition is found to be much more efficient in terms of time and yield. The&#xD;
structures of the newly synthesized compounds have been characterized by&#xD;
elemental analysis, IR and &lt;sup&gt;1&lt;/sup&gt;H NMR spectral data. All the newly&#xD;
synthesized compounds have been tested for their antibacterial properties&#xD;
against gram-positive and gram-negative bacteria.
&lt;br/&gt;
&lt;br/&gt;Page(s): 291-296</description>
      <pubDate>Thu, 29 Dec 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Synthesis of some new 3,4-disubstituted pyrroles and pyrazoles from &lt;i style="mso-bidi-font-style:normal"&gt;E&lt;/i&gt;-1-(arylsulfonylethylsulfonyl)-2-arylethene</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13404</link>
      <description>Title: Synthesis of some new 3,4-disubstituted pyrroles and pyrazoles from &lt;i style="mso-bidi-font-style:normal"&gt;E&lt;/i&gt;-1-(arylsulfonylethylsulfonyl)-2-arylethene
&lt;br/&gt;
&lt;br/&gt;Authors: Padmaja, A; Syamaiah, K; Muralikrishna, A; Padmavathi, V
&lt;br/&gt;
&lt;br/&gt;Abstract: The sulfonyl activated olefin, &lt;i style="mso-bidi-font-style:normal"&gt;E&lt;/i&gt;-1-(arylsulfonylethylsulfonyl)-2-arylethene&#xD;
&lt;b style="mso-bidi-font-weight:normal"&gt;7&lt;/b&gt; has been used as a synthon to&#xD;
develop a new class of pyrrole and pyrazole derivatives by 1,3-dipolar&#xD;
cycloaddition of TosMIC and diazomethane.
&lt;br/&gt;
&lt;br/&gt;Page(s): 285-290</description>
      <pubDate>Thu, 29 Dec 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Visibility and impact of the Indian Journal of Chemistry, Section B during 2005-2009 using scientometric techniques</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13403</link>
      <description>Title: Visibility and impact of the Indian Journal of Chemistry, Section B during 2005-2009 using scientometric techniques
&lt;br/&gt;
&lt;br/&gt;Authors: Nishy, P; Parvatharajan, Prema; Prathap, Gangan
&lt;br/&gt;
&lt;br/&gt;Abstract: Organic chemistry has&#xD;
always been one of the strongest areas of research in the chemical sciences in India.&#xD;
The Indian Journal of Chemistry, Section B is the leading journal from India&#xD;
covering important contributions in the area of organic and medicinal&#xD;
chemistry. This is the first attempt to carry out a scientometric assessment of&#xD;
the visibility and impact of this journal towards serving the needs of&#xD;
researchers, mainly from India,&#xD;
in these areas. All papers published in this journal during 2005 to 2009 have&#xD;
been analysed using various scientometric parameters like geographical&#xD;
distribution, citations received each year, authorship patterns, &lt;i style="mso-bidi-font-style:normal"&gt;etc&lt;/i&gt;. The papers are grouped under four&#xD;
main fields: (i) Heterocyclic Chemistry, (ii) Synthetic Organic Chemistry,&#xD;
(iii) Natural Products Chemistry and (iv) Theoretical Chemistry and assessment&#xD;
and performance of these and the forty five specialized sub-fields in organic&#xD;
chemistry have been studied.
&lt;br/&gt;
&lt;br/&gt;Page(s): 269-284</description>
      <pubDate>Thu, 29 Dec 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Mild, efficient and economical oxidative deprotection of allyl aryl ethers</title>
      <link>http://nopr.niscair.res.in/handle/123456789/13402</link>
      <description>Title: Mild, efficient and economical oxidative deprotection of allyl aryl ethers
&lt;br/&gt;
&lt;br/&gt;Authors: Lokhande, Pradeep D; Nawghare, Beena R
&lt;br/&gt;
&lt;br/&gt;Abstract: An efficient, economical&#xD;
procedure for the cleavage of allyl aryl ethers using a catalytic amount of&#xD;
iodine in dimethyl sulphoxide gives corresponding alcohols or phenols in high&#xD;
yields under mild condition. The reaction can be performed in air without loss&#xD;
of variety of oxidisable fuctional groups. Allyl ether of phenols is&#xD;
selectively deprotected in preference to alcohols. The reaction is highly&#xD;
regioselective and chemoselective.
&lt;br/&gt;
&lt;br/&gt;Page(s): 328-333</description>
      <pubDate>Thu, 29 Dec 2011 22:58:59 GMT</pubDate>
    </item>
  </channel>
</rss>

